Electreat, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Electreat, Inc. makes
Electreat, Inc. manufactures transcutaneous electrical stimulation devices, including the Model 250 Transcutaneous Stimulator and electrical nerve stimulators designed for therapeutic or diagnostic use.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Electreat Model 250 Transcutaneous Stim Ref K790189
Regimes: 510(k) Registry: 510(k)Stimulator, Electrical Nerve Ref K791158
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electreat, Inc. have in the registry?
The registry currently lists 2 devices for Electreat, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electreat, Inc.'s devices?
Among its 2 most recently registered devices, Electreat, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Electreat, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Electreat, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electreat, Inc. in the registry?
The most recently registered devices listed for Electreat, Inc. include ELECTREAT MODEL 250 TRANSCUTANEOUS STIM and STIMULATOR, ELECTRICAL NERVE.